CINGW

Cingulate Inc. Secures $5 Million Financing to Support Pharmaceutical Development Initiatives

Cingulate Inc. secures $5 million in financing to support clinical and operational activities, targeting NDA filing for CTx-1301 by mid-2025.

Quiver AI Summary

Cingulate Inc. has secured $5 million in net proceeds through a financing deal structured as a non-convertible, unsecured promissory note valued at $5.48 million, which will accrue interest at 9% per annum and matures in 18 months. The funds are intended for working capital and general corporate purposes, providing Cingulate with the necessary cash to support clinical, manufacturing, and regulatory activities through the fourth quarter of 2025. The company is targeting mid-2025 for the filing of its New Drug Application for potential FDA approval of its ADHD treatment, CTx-1301. This financing transaction is part of a private placement and does not involve registered securities under the Securities Act.

Potential Positives

  • Cingulate Inc. secured $5 million in net proceeds through a financing transaction, enhancing its financial stability and ability to support growth initiatives.
  • The funding provides Cingulate with a cash runway to support clinical, manufacturing, and regulatory activities, as well as operational costs, into the fourth quarter of 2025.
  • The company is targeting the filing of a New Drug Application (NDA) for potential FDA approval of CTx-1301 by mid-2025, indicating progress in its product development pipeline.

Potential Negatives

  • Completion of financing through a non-convertible, unsecured promissory note indicates potential cash flow challenges, raising concerns about the company's financial health.
  • The note's high interest rate of 9% per annum adds financial strain, which may impact future profitability and operational flexibility.
  • The press release highlights dependency on future financing or revenue generation to sustain operations beyond Q4 2025, which could signal uncertainty in the company's growth prospects.

FAQ

What recent financing transaction did Cingulate Inc. complete?

Cingulate Inc. completed a $5 million financing transaction through a non-convertible, unsecured promissory note.

How does Cingulate Inc. plan to use the proceeds from the financing?

The proceeds will be used for working capital and general corporate purposes, including clinical and regulatory activities.

What is the maturity period for the promissory note issued by Cingulate?

The promissory note matures 18 months after its issuance date.

What is the target date for the NDA submission for CTx-1301?

Cingulate aims to file the NDA for potential FDA approval of CTx-1301 in mid-2025.

What technology does Cingulate Inc. utilize in its drug development?

Cingulate utilizes its proprietary Precision Timed Release™ (PTR™) drug delivery platform for developing next-generation pharmaceuticals.

Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.


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Full Release



KANSAS CITY, Kan., Dec. 23, 2024 (GLOBE NEWSWIRE) --


Cingulate Inc.



(NASDAQ: CING)

, a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform technology to build and advance a pipeline of next-generation pharmaceutical products, has completed a financing transaction with an accredited investor which provided net proceeds to CING of $5 million. The transaction was structured as a non-convertible, unsecured promissory note in the principal amount of $5,480,000. The promissory note accumulates interest at a rate of 9% per annum and matures 18 months after its issuance date.



CING intends to use the net proceeds for working capital and other general corporate purposes. Based on planned expenditures, this additional capital provides CING the cash runway to fund clinical, manufacturing, and regulatory activities, as well as operating costs, into the fourth quarter of 2025. Filing of the NDA for potential FDA approval of CTx-1301 is targeted for mid-2025.



The offer and sale of the promissory note is being made by Cingulate Inc. in a private placement under Section 4(a)(2) of the Securities Act of 1933, as amended, and/or Regulation D promulgated thereunder, and such securities have not been registered under the Act or applicable state securities laws. Accordingly, such securities may not be offered or sold in the United States except pursuant to an effective registration statement or an applicable exemption from the registration requirements of the Act and such applicable state securities laws.



This press release shall not constitute an offer to sell or a solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.




About Cingulate Inc.



Cingulate Inc. (Nasdaq: CING), is a biopharmaceutical company utilizing its proprietary PTR drug delivery platform technology to build and advance a pipeline of next-generation pharmaceutical products, designed to improve the lives of patients suffering from frequently diagnosed conditions characterized by burdensome daily dosing regimens and suboptimal treatment outcomes. With an initial focus on the treatment of ADHD, Cingulate is identifying and evaluating additional therapeutic areas where PTR technology may be employed to develop future product candidates, including to treat anxiety disorders. Cingulate is headquartered in Kansas City.




Forward-Looking Statements



This press release contains “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements include all statements, other than statements of historical fact, regarding our current views and assumptions with respect to future events regarding our business, including statements with respect to our plans, assumptions, expectations, beliefs and objectives with respect to product development, clinical studies, clinical and regulatory timelines, market opportunity, competitive position, business strategies, potential growth opportunities and other statements that are predictive in nature. These statements are generally identified by the use of such words as “may,” “could,” “should,” “would,” “believe,” “anticipate,” “forecast,” “estimate,” “expect,” “intend,” “plan,” “continue,” “outlook,” “will,” “potential” and similar statements of a future or forward-looking nature. Readers are cautioned that any forward-looking information provided by us or on our behalf is not a guarantee of future performance. Actual results may differ materially from those contained in these forward-looking statements as a result of various factors disclosed in our filings with the Securities and Exchange Commission (SEC), including the “Risk Factors” section of our Annual Report on Form 10-K filed with the SEC on April 1, 2024 and our other filings with the SEC. All forward-looking statements speak only as of the date on which they are made, and we undertake no duty to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except to the extent required by law.




Investor & Public Relations:



Thomas Dalton


Vice President, Investor & Public Relations, Cingulate




tdalton@cingulate.com






(913) 942-2301



Matt Kreps


Darrow Associates




mkreps@darrowir.com






(214) 597-8200






This article was originally published on Quiver News, read the full story.

The views and opinions expressed herein are the views and opinions of the author and do not necessarily reflect those of Nasdaq, Inc.

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